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rs2278702

From SNPedia

Orientationminus
Stabilizedminus
Make rs2278702(A;A)
Make rs2278702(A;T)
Make rs2278702(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position80402580
GeneARNT2, LOC101929560
is asnp
is mentioned by
dbSNPrs2278702
ebirs2278702
HLIrs2278702
Exacrs2278702
Varsomers2278702
Maprs2278702
PheGenIrs2278702
hapmaprs2278702
1000 genomesrs2278702
hgdprs2278702
ensemblrs2278702
gopubmedrs2278702
geneviewrs2278702
scholarrs2278702
googlers2278702
pharmgkbrs2278702
gwascentralrs2278702
openSNPrs2278702
23andMers2278702
23andMe allrs2278702
SNP Nexus

SNPshotrs2278702
SNPdbers2278702
MSV3drs2278702
GWAS Ctlgrs2278702
GMAF0.2259
Max Magnitude
? (A;A) (A;T) (T;T) 28
GWAS snp
PMID [PMID 18711365OA-icon.png]
Trait Bipolar disorder
Title Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder
Risk Allele
P-val 0.0000060000000000000002
Odds Ratio 1.21 [NR]


GET Evidence
rs2278702
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.21875
summary